Copper-treatment increases the cellular GSH content and accelerates GSH export from cultured rat astrocytes

被引:45
作者
Scheiber, Ivo F. [1 ,2 ]
Dringen, Ralf [1 ,2 ,3 ]
机构
[1] Univ Bremen, Ctr Biomol Interact Bremen, D-28334 Bremen, Germany
[2] Ctr Environm Res & Sustainable Technol, D-28359 Bremen, Germany
[3] Monash Univ, Sch Psychol & Psychiat, Clayton, Vic 3800, Australia
关键词
Astrocytes; Copper; Glutathione; Mrp1; Transport; ASTROGLIAL CELLS; GLUTATHIONE EFFLUX; OXIDATIVE STRESS; WILSONS-DISEASE; NITRIC-OXIDE; IN-VIVO; BRAIN; METABOLISM; TOXICITY; ACCUMULATION;
D O I
10.1016/j.neulet.2011.04.058
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
To test whether copper exposure affects astroglial glutathione (GSH) metabolism, we have exposed astrocyte-rich primary cultures with copper chloride in concentrations of up to 30 mu M and investigated cellular and extracellular GSH contents. Cultured astrocytes accumulated copper in a concentration-dependent manner thereby increasing the specific cellular copper content within 24 h up to sevenfold. The increase in the cellular copper content was accompanied by a proportional increase in the specific cellular GSH content that reached up to 165% of the values of cells that had been incubated without copper, while the low cellular content of GSH disulfide (GSSG) remained unaltered in copper-treated cells. Also the rate of GSH export was significantly increased after copper exposure reaching up to 177% of control values. The export of GSH from control and copper-treated astrocytes was lowered by more than 70%, if cells were incubated in presence of the multidrug-resistance protein (Mrp) 1 inhibitor MK571 or at a low incubation temperature of 4 degrees C. These data demonstrate that copper accumulation stimulates GSH synthesis and accelerates Mrp1-mediated GSH export from cultured astrocytes. These processes are likely to contribute to the resistance of astrocytes against copper toxicity and could improve the supply of GSH precursors from astrocytes to neurons. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:42 / 46
页数:5
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